The trial was designed with a 72-week treatment duration plus a follow-off period, giving it a projected primary completion date in late 2025 to early 2026
And the FDA has received reports of adverse events, including some requiring hospitalization, related to dosing errors with compounded semaglutide
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Resources Honda, Yasushi, et al
Common adverse effects include gastrointestinal symptoms, like nausea, vomiting, and diarrhea, but rare risks such as pancreatitis or thyroid tumors have been reported